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Effect of booster vaccination against Delta and Omicron SARS-CoV-2 variants in Iceland.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33076-4
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- Publication type:
- Article
Polygenic risk scores for schizophrenia and bipolar disorder associate with addiction.
- Published in:
- 2018
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- Publication type:
- journal article
Obesity Variants in the GIPR Gene Are not Associated With Risk of Fracture or Bone Mineral Density.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2024, v. 109, n. 8, p. e1608, doi. 10.1210/clinem/dgad734
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- Publication type:
- Article
Predicting the probability of death using proteomics.
- Published in:
- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02289-6
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- Publication type:
- Article
Loss-of-function variants in ATM confer risk of gastric cancer.
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- Nature Genetics, 2015, v. 47, n. 8, p. 906, doi. 10.1038/ng.3342
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- Publication type:
- Article
Identification of a large set of rare complete human knockouts.
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- Nature Genetics, 2015, v. 47, n. 5, p. 448, doi. 10.1038/ng.3243
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- Publication type:
- Article
Large-scale whole-genome sequencing of the Icelandic population.
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- Nature Genetics, 2015, v. 47, n. 5, p. 435, doi. 10.1038/ng.3247
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- Publication type:
- Article
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.
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- Nature Genetics, 2014, v. 46, n. 8, p. 826, doi. 10.1038/ng.3014
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- Publication type:
- Article
Common and low-frequency variants associated with genome-wide recombination rate.
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- Nature Genetics, 2014, v. 46, n. 1, p. 11, doi. 10.1038/ng.2833
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- Publication type:
- Article
A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration.
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- Nature Genetics, 2013, v. 45, n. 11, p. 1371, doi. 10.1038/ng.2740
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- Publication type:
- Article
A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer.
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- Nature Genetics, 2012, v. 44, n. 12, p. 1326, doi. 10.1038/ng.2437
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- Publication type:
- Article
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.
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- Nature Genetics, 2012, v. 44, n. 3, p. 260, doi. 10.1038/ng.1051
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- Publication type:
- Article
Discovery of common variants associated with low TSH levels and thyroid cancer risk.
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- Nature Genetics, 2012, v. 44, n. 3, p. 319, doi. 10.1038/ng.1046
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- Publication type:
- Article
Mutations in BRIP1 confer high risk of ovarian cancer.
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- Nature Genetics, 2011, v. 43, n. 11, p. 1104, doi. 10.1038/ng.955
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- Publication type:
- Article
A germline variant in the TP53 polyadenylation signal confers cancer susceptibility.
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- Nature Genetics, 2011, v. 43, n. 11, p. 1098, doi. 10.1038/ng.926
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- Publication type:
- Article
Identification of low-frequency variants associated with gout and serum uric acid levels.
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- Nature Genetics, 2011, v. 43, n. 11, p. 1127, doi. 10.1038/ng.972
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- Publication type:
- Article
A rare variant in MYH6 is associated with high risk of sick sinus syndrome.
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- Nature Genetics, 2011, v. 43, n. 4, p. 316, doi. 10.1038/ng.781
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- Publication type:
- Article
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.
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- Nature Genetics, 2010, v. 42, n. 12, p. 1077, doi. 10.1038/ng.714
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- Publication type:
- Article
Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior.
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- Nature Genetics, 2010, v. 42, n. 5, p. 448, doi. 10.1038/ng.573
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- Publication type:
- Article
A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.
- Published in:
- Nature Genetics, 2010, v. 42, n. 5, p. 415, doi. 10.1038/ng.558
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- Publication type:
- Article
Several common variants modulate heart rate, PR interval and QRS duration.
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- Nature Genetics, 2010, v. 42, n. 2, p. 117, doi. 10.1038/ng.511
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- Publication type:
- Article
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.
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- Nature Genetics, 2009, v. 41, n. 10, p. 1122, doi. 10.1038/ng.448
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- Publication type:
- Article
New common variants affecting susceptibility to basal cell carcinoma.
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- Nature Genetics, 2009, v. 41, n. 8, p. 909, doi. 10.1038/ng.412
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- Publication type:
- Article
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
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- Nature Genetics, 2009, v. 41, n. 8, p. 876, doi. 10.1038/ng.417
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- Publication type:
- Article
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.
- Published in:
- Nature Genetics, 2009, v. 41, n. 8, p. 926, doi. 10.1038/ng.404
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- Publication type:
- Article
Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche.
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- Nature Genetics, 2009, v. 41, n. 6, p. 734, doi. 10.1038/ng.383
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- Publication type:
- Article
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations.
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- Nature Genetics, 2009, v. 41, n. 4, p. 460, doi. 10.1038/ng.339
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- Publication type:
- Article
New sequence variants associated with bone mineral density.
- Published in:
- Nature Genetics, 2009, v. 41, n. 1, p. 15, doi. 10.1038/ng.284
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- Publication type:
- Article
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.
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- Nature Genetics, 2009, v. 41, n. 1, p. 18, doi. 10.1038/ng.274
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- Publication type:
- Article
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits.
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- Nature Genetics, 2008, v. 40, n. 11, p. 1313, doi. 10.1038/ng.234
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- Publication type:
- Article
Detection of sharing by descent, long-range phasing and haplotype imputation.
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- Nature Genetics, 2008, v. 40, n. 9, p. 1068, doi. 10.1038/ng.216
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- Publication type:
- Article
Corrigendum: ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.
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- 2008
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- Publication type:
- Correction Notice
ASIP and TYR pigmentation variants associate with cutaneous melanoma and basal cell carcinoma.
- Published in:
- Nature Genetics, 2008, v. 40, n. 7, p. 886, doi. 10.1038/ng.161
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- Publication type:
- Article
Two newly identified genetic determinants of pigmentation in Europeans.
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- Nature Genetics, 2008, v. 40, n. 7, p. 835, doi. 10.1038/ng.160
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- Publication type:
- Article
Many sequence variants affecting diversity of adult human height.
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- Nature Genetics, 2008, v. 40, n. 5, p. 609, doi. 10.1038/ng.122
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- Publication type:
- Article
Genetic determinants of hair, eye and skin pigmentation in Europeans.
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- Nature Genetics, 2007, v. 39, n. 12, p. 1443, doi. 10.1038/ng.2007.13
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- Publication type:
- Article
A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction.
- Published in:
- Nature Genetics, 2006, v. 38, n. 1, p. 68, doi. 10.1038/ng1692
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- Publication type:
- Article
Allegro version 2.
- Published in:
- 2005
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- Publication type:
- Letter
A common inversion under selection in Europeans.
- Published in:
- Nature Genetics, 2005, v. 37, n. 2, p. 129, doi. 10.1038/ng1508
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- Publication type:
- Article
Recombination rate and reproductive success in humans.
- Published in:
- Nature Genetics, 2004, v. 36, n. 11, p. 1203, doi. 10.1038/ng1445
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- Publication type:
- Article
A high-resolution recombination map of the human genome.
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- Nature Genetics, 2002, v. 31, n. 3, p. 241, doi. 10.1038/ng917
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- Publication type:
- Article
Allegro, a new computer program for multipoint linkage analysis.
- Published in:
- Nature Genetics, 2000, v. 25, n. 1, p. 12, doi. 10.1038/75514
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- Publication type:
- Article
COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA.
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- 2017
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- Publication type:
- Case Study
Compound heterozygous mutations in UBA5 causing early-onset epileptic encephalopathy in two sisters.
- Published in:
- 2017
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- Publication type:
- Case Study
Age and Influenza-Specific Pre-Vaccination Antibodies Strongly Affect Influenza Vaccine Responses in the Icelandic Population whereas Disease and Medication Have Small Effects.
- Published in:
- Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2017.01872
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- Publication type:
- Article
Predicting the presence of coronary plaques featuring high-risk characteristics using polygenic risk scores and targeted proteomics in patients with suspected coronary artery disease.
- Published in:
- Genome Medicine, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13073-024-01313-8
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- Publication type:
- Article
European Bone Mineral Density Loci Are Also Associated with BMD in East-Asian Populations.
- Published in:
- PLoS ONE, 2010, v. 5, n. 10, p. 1, doi. 10.1371/journal.pone.0013217
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- Publication type:
- Article
GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-13341-9
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- Publication type:
- Article
Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-09304-9
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- Publication type:
- Article
Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-018-08107-8
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- Publication type:
- Article